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2005
OMIG, Abstract 20
OMIG
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0.005% Benzalkonium Chloride
(BAK): Is it Effective in Eliminating Staphylococcus aureus
and Pseudomonas aeruginosa?
R.P. Kowalski, B.R. Kowalski, P.P. Thompson, E.G.
Romanowski, F.S. Mah, Y.J. Gordon. The Charles T. Campbell Laboratory,
University of Pittsburgh, Pittsburgh, PA
Purpose. We determined the in vitro
efficacy of 0.005% BAK as a biocide alone, and with moxifloxacin
(MOX) and gatifloxacin (GAT) to eliminate Staphylococus aureus
and Pseudomonas aeruginosa.
Methods. Standard time-kill studies
were determined with 5 isolates each of Staphylococcus aureus
and Pseudomonas aeruginosa. Bacteria survival was tested
at hours 1, 2, 4, 6, 8 and 24 hours to: 1) vehicle (Mueller Hinton
broth), 2) 0.005% [50 ug/ml] BAK, 3) 0.5% MOX, 4) 0.3% GAT, 5) 0.3%
GAT + 0.005% BAK, and-6) 0.5% MOX + 0.005% BAK. The initial inoculum
was 1 x 106 cm/ml. The MICs of all the isolates were determined
to BAK using the broth dilution method.
Results. For Staphylococcus aureus,
0.005% BAK, 0.3 % GAT + 0.005% BAK, and 0.5% MOX + 0.005% BAK eliminated
all growth within 1 hour. 0.3% GAT + 0.005% BAK (median 1 hr) eliminated
bacteria faster than 0.5% MOX (median 4 hrs) (p=0.016). The MICs
to BAK ranged from 1 to 8 ug/ml. For Pseudomonas aeruginosa,
0.005% BAK had no eliminating effect. 0.3% GAT, 0.5% MOX, 0.3% GAT
+ 0.005% BAK, and 0.5% MOX + 0.005% BAK eliminated all growth within
1 hour. The MICs to BAK ranged from 64 to >128 ug/ml.
Conclusions. 0.005% BAK appears to
complement GAT for eliminating Staphylococcus aureus while
it has no effect on Pseudomonas aeruginosa. GAT and MOX
appear to act as self-preservatives against P. aeruginosa.
It is possible that BAK (depending on concentration) may not preserve
all topical ocular non-antibiotic medications against P. aeruginosa.
Disclosure code: N
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